Variant (rsID / SNP)

rs76737438

rs76737438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ1. Location: chromosome 11, position 2,591,916. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

KCNQ1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:2591916
Cytoband: 11p15.5
HGVS: NM_000218.3(KCNQ1):c.536G>C (p.Gly179Ala)
Allele change: Missense_G179A

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.